| Literature DB >> 29602394 |
Guanshi Zhang1, Manjula Darshi1, Kumar Sharma2.
Abstract
Diabetic kidney disease (DKD) is the leading cause of morbidity and mortality in diabetic patients. Defining risk factors for DKD using a reductionist approach has proven challenging. Integrative omics-based systems biology tools have shed new insights in our understanding of DKD and have provided several key breakthroughs for identifying novel predictive and diagnostic biomarkers. In this review, we highlight the role of the Warburg effect in DKD and potential regulating factors such as sphingomyelin, fumarate, and pyruvate kinase muscle isozyme M2 in shifting glucose flux from complete oxidation in mitochondria to the glycolytic pathway and its principal branches. With the development of highly sensitive instruments and more advanced automatic bioinformatics tools, we believe that omics analyses and imaging techniques will focus more on singular-cell-level studies, which will allow in-depth understanding of DKD and pave the path for personalized kidney precision medicine. Published by Elsevier Inc.Entities:
Keywords: Diabetic kidney disease; aerobic glycolysis; metabolomics; mitochondrion; the Warburg effect
Mesh:
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Year: 2018 PMID: 29602394 PMCID: PMC5973839 DOI: 10.1016/j.semnephrol.2018.01.002
Source DB: PubMed Journal: Semin Nephrol ISSN: 0270-9295 Impact factor: 5.299